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Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients.
Erfanian Omidvar, Maryam; Torkamandi, Shahram; Rezaei, Somaye; Alipoor, Behnam; Omrani, Mir Davood; Darvish, Hossein; Ghaedi, Hamid.
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  • Erfanian Omidvar M; Department of Medical Laboratory Technology, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Torkamandi S; Department of Medical Genetics and Immunology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
  • Rezaei S; Department of Neurology, Imam Khomeini Hospital, Urmia University of Medical Sciences, Urmia, Iran.
  • Alipoor B; Department of Laboratory Sciences, Faculty of Parmedicine, Yasuj University of Medical Sciences, Yasuj, Iran.
  • Omrani MD; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Velenjak St., Shahid Chamran Highway, Tehran, IR, Iran.
  • Darvish H; Department of Medical Genetics, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Ghaedi H; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Velenjak St., Shahid Chamran Highway, Tehran, IR, Iran. h.qaedi@sbmu.ac.ir.
J Neurol ; 268(6): 2065-2082, 2021 Jun.
Article en En | MEDLINE | ID: mdl-31745725
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Risk_factors_studies / Systematic_reviews Límite: Adult / Humans / Male Idioma: En Revista: J Neurol Año: 2021 Tipo del documento: Article País de afiliación: Irán
Texto completo
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PubMed Links
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Risk_factors_studies / Systematic_reviews Límite: Adult / Humans / Male Idioma: En Revista: J Neurol Año: 2021 Tipo del documento: Article País de afiliación: Irán